Canonical Allele Identifier: CA2260099647
Gene: KRT16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41612224C= , CM000679.2:g.41612224C= GRCh38
NC_000017.10:g.39768476C= , CM000679.1:g.39768476C= GRCh37
NC_000017.9:g.37022002C= NCBI36
NG_008301.1:g.5604G=

Transcript Alleles

HGVS Amino-acid change
ENST00000301653.9:c.465G= MANE Select ENSP00000301653.3:p.Arg155=
ENST00000301653.8:c.465G= ENSP00000301653.3:p.Arg155=
ENST00000588319.1:n.542G=
ENST00000593067.1:c.-250G= ENSP00000467124.1:n.-250G=
NM_005557.3:c.465G= NP_005548.2:p.Arg155=
NM_005557.4:c.465G= MANE Select NP_005548.2:p.Arg155=